The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function
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The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function
The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function
解放军医学杂志(英文版)1992年第3期 页码:265-268
Affiliations:
1. Department of Pharmacology First Military Medical University
2. ,Guangzhou,510515
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纸质出版:1992
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The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function[J]. 解放军医学杂志(英文版), 1992,(3):265-268.
[1]龚剑平,龚彦德,刘菊芳,张永胜.The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function[J].Journal of Medical Colleges of PLA,1992(03):265-268.
The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function[J]. 解放军医学杂志(英文版), 1992,(3):265-268.DOI:
[1]龚剑平,龚彦德,刘菊芳,张永胜.The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function[J].Journal of Medical Colleges of PLA,1992(03):265-268.DOI:
The effects of scorpion(Buthus martensi Karsch)venom on rat left ventricular function
摘要
Abstract
<正> In order to investigate the cardiovascular effects of the scorpion(Buthus martensiKarsch)venom(BmKv)
the left ventricle of the rats was catheterized via the right carotidartery.The LVP
LVEDP
+dp/dt max
Vmax
HR and BP were observed.The results showedthat intravenous injection of the BmKv(60μg/kg)
in comparison with the control
elicited obvi-ous hypertension and increase of cardiac contractility
both of which lasted for 1h
while theheart rate had no significant change rand that pretreating the rats with alpha-adrenergic blocker
phentolamine
antagonized the hypertensive effects
but did not antagonize the increase of cardiaccontractility.Pretreatment with beta-adrenergic blocker
propranolol
has no influence on the ef-fects of the venom.It is suggested that the hypertensive effects are due to the activation of al-pha-adrenergic receptor
whereas the increase of cardiac contractility may not be resulted fromthe activation of beta-adrenergic receptor.The BmKv treated with dithiothreitol before injectionhad no cardiovascular effects
indicating that the intact disulfide bridges play a decisive role inthe cardiovascular effects of the BmKv.
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